Short tandem repeat polymorphisms in Japanese families with phenylketonuria.

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作者信息

Kang Y, Okano Y, Hase Y, Oura T, Isshiki G

机构信息

Department of Pediatrics, National Sengokusou Hospital, Kaizuka, Japan.

出版信息

J Inherit Metab Dis. 1996;19(3):375-6. doi: 10.1007/BF01799274.

DOI:10.1007/BF01799274

PMID:8803787

Abstract

摘要

相似文献

Short tandem repeat polymorphisms in Japanese families with phenylketonuria.

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本文引用的文献

Mutation of human short tandem repeats.

Hum Mol Genet. 1993 Aug;2(8):1123-8. doi: 10.1093/hmg/2.8.1123.

A single polymorphic STR system in the human phenylalanine hydroxylase gene permits rapid prenatal diagnosis and carrier screening for phenylketonuria.

Hum Mol Genet. 1993 May;2(5):577-81. doi: 10.1093/hmg/2.5.577.

A simple, rapid, and highly informative PCR-based procedure for prenatal diagnosis and carrier screening of phenylketonuria.

Prenat Diagn. 1994 Dec;14(12):1113-8. doi: 10.1002/pd.1970141204.

Frequency and distribution of phenylketonuric mutations in Orientals.

Hum Mutat. 1992;1(3):216-20. doi: 10.1002/humu.1380010307.

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